Package 80425-0422-1

{"route": ["ORAL"], "spl_id": "1d625438-34dd-fbba-e063-6294a90afd2f", "openfda": {"nui": ["N0000000151", "N0000175784", "N0000000160", "M0001335", "N0000175722"], "unii": ["5QZO15J2Z8", "WK2XYI10QM"], "rxcui": ["1100066"], "spl_set_id": ["1d625438-34dc-fbba-e063-6294a90afd2f"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]", "Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0422-1)", "package_ndc": "80425-0422-1", "marketing_start_date": "20240716"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0422-2)", "package_ndc": "80425-0422-2", "marketing_start_date": "20240716"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (80425-0422-3)", "package_ndc": "80425-0422-3", "marketing_start_date": "20240716"}], "brand_name": "Ibuprofen and famotidine", "product_id": "80425-0422_1d625438-34dd-fbba-e063-6294a90afd2f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "80425-0422", "generic_name": "Ibuprofen and famotidine", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen and famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "26.6 mg/1"}, {"name": "IBUPROFEN", "strength": "800 mg/1"}], "application_number": "ANDA211890", "marketing_category": "ANDA", "marketing_start_date": "20240716", "listing_expiration_date": "20261231"}